Author
Listed:
- Jiangming Sun
(Mental Health Center Sct. Hans, Mental Health Services Copenhagen
The Lundbeck Foundation Initiative for Integrative Psychiatric Research (iPSYCH)
Malmö, Lund University)
- Yunpeng Wang
(University of Oslo)
- Lasse Folkersen
(Mental Health Center Sct. Hans, Mental Health Services Copenhagen
The Lundbeck Foundation Initiative for Integrative Psychiatric Research (iPSYCH))
- Yan Borné
(Malmö, Lund University)
- Inge Amlien
(University of Oslo)
- Alfonso Buil
(Mental Health Center Sct. Hans, Mental Health Services Copenhagen
The Lundbeck Foundation Initiative for Integrative Psychiatric Research (iPSYCH))
- Marju Orho-Melander
(Malmö, Lund University)
- Anders D. Børglum
(The Lundbeck Foundation Initiative for Integrative Psychiatric Research (iPSYCH)
Human Genetics and Centre for Integrative Sequencing, Aarhus University)
- David M. Hougaard
(The Lundbeck Foundation Initiative for Integrative Psychiatric Research (iPSYCH)
Center for Neonatal Screening, Statens Serum Institut)
- Olle Melander
(Malmö, Lund University)
- Gunnar Engström
(Malmö, Lund University)
- Thomas Werge
(Mental Health Center Sct. Hans, Mental Health Services Copenhagen
The Lundbeck Foundation Initiative for Integrative Psychiatric Research (iPSYCH)
University of Copenhagen)
- Kasper Lage
(Mental Health Center Sct. Hans, Mental Health Services Copenhagen
Stanley Center at Broad Institute of MIT and Harvard
Massachusetts General Hospital)
Abstract
A promise of genomics in precision medicine is to provide individualized genetic risk predictions. Polygenic risk scores (PRS), computed by aggregating effects from many genomic variants, have been developed as a useful tool in complex disease research. However, the application of PRS as a tool for predicting an individual’s disease susceptibility in a clinical setting is challenging because PRS typically provide a relative measure of risk evaluated at the level of a group of people but not at individual level. Here, we introduce a machine-learning technique, Mondrian Cross-Conformal Prediction (MCCP), to estimate the confidence bounds of PRS-to-disease-risk prediction. MCCP can report disease status conditional probability value for each individual and give a prediction at a desired error level. Moreover, with a user-defined prediction error rate, MCCP can estimate the proportion of sample (coverage) with a correct prediction.
Suggested Citation
Jiangming Sun & Yunpeng Wang & Lasse Folkersen & Yan Borné & Inge Amlien & Alfonso Buil & Marju Orho-Melander & Anders D. Børglum & David M. Hougaard & Olle Melander & Gunnar Engström & Thomas Werge &, 2021.
"Translating polygenic risk scores for clinical use by estimating the confidence bounds of risk prediction,"
Nature Communications, Nature, vol. 12(1), pages 1-9, December.
Handle:
RePEc:nat:natcom:v:12:y:2021:i:1:d:10.1038_s41467-021-25014-7
DOI: 10.1038/s41467-021-25014-7
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